List of variants reported as pathogenic for autosomal dominant nonsyndromic hearing loss 4A by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys)	rs119103280	0.00303
NM_001145809.2(MYH14):c.20C>A (p.Ser7Ter)	rs119103279
NM_001145809.2(MYH14):c.2299C>A (p.Arg767Ser)	rs28940307
NM_001145809.2(MYH14):c.3049C>T (p.Leu1017Phe)	rs28940306
NM_001145809.2(MYH14):c.359C>T (p.Ser120Leu)	rs119103281

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